Canonical Allele Identifier: PA2828048394
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299898
ClinVar RCV Id: RCV000272691 RCV000307731 RCV000362457 RCV000393505 RCV001015632 RCV002520586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gly569Arg
CA10635707
NM_001355216.1:c.1705G>A
CA376556286
NM_001355216.1:c.1705G>C